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对羟基苯甲黄嘌呤和咖啡因对人体的拟交感神经作用。

Sympathomimetic effects of paraxanthine and caffeine in humans.

作者信息

Benowitz N L, Jacob P, Mayan H, Denaro C

机构信息

Clinical Pharmacology Unit, San Francisco General Hospital Medical Center, USA.

出版信息

Clin Pharmacol Ther. 1995 Dec;58(6):684-91. doi: 10.1016/0009-9236(95)90025-X.

Abstract

Caffeine is metabolized extensively (on average 80%) to paraxanthine. With regular caffeine consumption, average serum levels of paraxanthine are two thirds those of caffeine. Both caffeine and paraxanthine competitively and nonselectively inhibit adenosine receptors in vitro. To examine the contribution of paraxanthine to the pharmacologic activity of caffeine, we administered to 12 subjects in a crossover design oral caffeine (2 or 4 mg/kg) versus placebo or oral paraxanthine (same dose as caffeine) versus placebo, each after 3 days of methylxanthine abstinence. Both caffeine and paraxanthine significantly increased diastolic blood pressure, plasma epinephrine levels, and free fatty acids. Caffeine and paraxanthine produced a similar magnitude of response at 4 mg/kg; however, caffeine appeared to produce greater responses than paraxanthine at 2 mg/kg. Caffeine and paraxanthine have similar sympathomimetic actions. The activity of paraxanthine needs to be considered in understanding the clinical pharmacology of caffeine, particularly with chronic, repetitive caffeine consumption.

摘要

咖啡因大部分(平均80%)代谢为对黄嘌呤。经常摄入咖啡因时,对黄嘌呤的平均血清水平是咖啡因的三分之二。咖啡因和对黄嘌呤在体外均能竞争性、非选择性地抑制腺苷受体。为研究对黄嘌呤对咖啡因药理活性的作用,我们采用交叉设计,让12名受试者在戒断甲基黄嘌呤3天后,分别口服咖啡因(2或4mg/kg)与安慰剂,或口服对黄嘌呤(与咖啡因剂量相同)与安慰剂。咖啡因和对黄嘌呤均显著升高舒张压、血浆肾上腺素水平及游离脂肪酸。4mg/kg时,咖啡因和对黄嘌呤产生的反应幅度相似;然而,2mg/kg时,咖啡因产生的反应似乎比对黄嘌呤更大。咖啡因和对黄嘌呤具有相似的拟交感神经作用。在理解咖啡因的临床药理学时,尤其是对于长期、重复摄入咖啡因的情况,需要考虑对黄嘌呤的活性。

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